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(1R,2S)-1-(2,5-Dimethoxy-benzyl)-1,2,5,5-tetramethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene is a complex organic compound with a molecular formula of C21H28O2. It features a naphthalene core, which is a type of polycyclic aromatic hydrocarbon, and is modified with a 2,5-dimethoxy-benzyl group attached to the 1-position. The molecule also has four methyl groups attached to the 1, 2, 5, and 5 positions, respectively. The stereochemistry of the molecule is defined by the (1R,2S) configuration, indicating the specific three-dimensional arrangement of the atoms around the chiral centers. (1R,2S)-1-(2,5-Dimethoxy-benzyl)-1,2,5,5-tetramethyl-1,2,3,4,5,6,7,8-octahydro-naphthalene is likely to be found in the field of organic chemistry, potentially as a synthetic intermediate or a component in pharmaceuticals or other chemical industries, due to its unique structure and functional groups.

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72853-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72853-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,5 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72853-86:
(7*7)+(6*2)+(5*8)+(4*5)+(3*3)+(2*8)+(1*6)=152
152 % 10 = 2
So 72853-86-2 is a valid CAS Registry Number.

72853-86-2Downstream Products

72853-86-2Relevant academic research and scientific papers

A six-step synthetic approach to marine natural product (+)-aureol

Wang, Jun-Li,Li, Hui-Jing,Wang, Meirong,Wang, Jun-Hu,Wu, Yan-Chao

, p. 945 - 948 (2018/02/09)

A concise synthetic approach to the marine natural product (+)-aureol has been achieved from readily available starting materials using obviously fewer steps in comparison to the related report in literature (6 steps versus 12 steps from (+)-sclareolide). Key steps of this protocol include a boron trifluoride-catalyzed domino 1,2-H and 1,2-methyl shifts and a nickel(II)-catalyzed cross-coupling reaction between an alkyl iodide and an aryl Grignard reagent.

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